Canonical Allele Identifier: CA1583233444

Gene: RAD50

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132618038_132618039delinsTG , CM000667.2:g.132618038_132618039delinsTG	GRCh38
NC_000005.9:g.131953730_131953731delinsTG , CM000667.1:g.131953730_131953731delinsTG	GRCh37
NC_000005.8:g.131981629_131981630delinsTG	NCBI36
NG_021151.1:g.66115_66116delinsTG
NG_021151.2:g.66062_66063delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378823.8:c.3165-32_3165-31delinsTG MANE Select	ENSP00000368100.4:n.3165-32_3165-31delinsTG
ENST00000638452.2:c.2868-32_2868-31delinsTG	ENSP00000492349.2:n.2868-32_2868-31delinsTG
ENST00000638504.1:n.2773-32_2773-31delinsTG
ENST00000638568.2:c.2868-32_2868-31delinsTG	ENSP00000491158.2:n.2868-32_2868-31delinsTG
ENST00000639899.1:n.3684-32_3684-31delinsTG
ENST00000640655.2:c.2868-32_2868-31delinsTG	ENSP00000491596.2:n.2868-32_2868-31delinsTG
ENST00000378823.7:c.3165-32_3165-31delinsTG	ENSP00000368100.4:n.3165-32_3165-31delinsTG
ENST00000533482.5:c.*2791-32_*2791-31delinsTG	ENSP00000431225.1:n.*2791-32_*2791-31delinsTG
NM_005732.3:c.3165-32_3165-31delinsTG	NP_005723.2:n.3165-32_3165-31delinsTG
NM_005732.4:c.3165-32_3165-31delinsTG MANE Select	NP_005723.2:n.3165-32_3165-31delinsTG